Heart Failure Precision Medicine Study with Telemonitoring

This study is looking for 100 people with heart failure to understand how different molecular profiles (multi-omics studies) relate to heart failure outcomes. It also aims to see if using telemonitoring devices (heart rate and blood pressure monitor, scale, and activity tracker) can help doctors optimize your treatment. You can join if you have a heart failure diagnosis, objective evidence of a heart abnormality (like an abnormal ECHO or high B-type natriuretic peptide levels over 100 pg/ml), and are between 21 and older. The main goal is to track adverse outcomes related to heart failure over five years. The current status of the study is unclear.

Study design
This is an interventional study planning to enroll 100 participants. It involves a randomized telemonitoring intervention.
What's involved
You would need to be able to use a smartphone to participate. The study will involve longitudinal profiling based on clinical data and multi-omics profiling.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for five years from enrollment to measure adverse outcomes.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT04196842

Heart Failure Precision Medicine Study

Recruiting
NAAges 21+InterventionalSupportive care
University of California, Davis
~100 participants
Updated 2026-02-09 on ClinicalTrials.gov
What's tested:Telemonitoring devices

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Rate of adverse outcomes in heart failure
Measured over Five years from enrollment
Heart Failure

NCT04196842

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • UC Davis Medical Center

    Sacramento, Californiastudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Martin Cadeiras, MD · PRINCIPAL_INVESTIGATOR · University of California, Davis

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Eligibility criteria

Inclusion

Diagnosis of Heart failure
Objective evidence of cardiac abnormality of structure or function (abnormal ECHO) or elevated levels of B-type natriuretic peptide (\>100 pg/ml)
HF stage B-D and class I-IV

Exclusion

Patients unable to consent
Inability to comply with the protocol and follow-up requirements
Patients unable to use a smartphone
Patients assessed irregularly (less than two visits in one year)
History of HTx
Use of Mechanical circulatory support device (MCSD)
Comorbidities that, according to the PI, have the potential to interfere with the interpretation of the results
  • Rate of adverse outcomes in heart failureFive years from enrollment

    Rate of Mortality (all cause), hospitalization, Mechanical circulatory support device (MCSD) or heart transplant (HTx)